Saturday, 11 May 2013

AYRTON Drug Seeks Regulatory Affairs Executive

AYRTON Drug has job opportunities in Ghana to recruit Regulatory Affairs Executive. We were incorporated On the 24th September 1965 by the Late Mr. Samuel Benson Adjapong. As a Ghanaian Entrepreneur and the first Ghanaian Chief Pharmacist at the Ministry of Health; he was issued a certificate to commence business on 21st October 1965. The company's journey to stardom began in a small plant in Kokomlemle a suburb of Accra with a tablet making machine and a staff of ten(10). It moved to its current location on the Abeka Road, Tesano also in Accra in 1969.

During the years 1970-1982, when many manufacturing companies in Ghana were operating on the margin due to the harsh economic conditions, Ayrton kept alive the hope of becoming a force in the pharmaceutical industry in Ghana with a about 30 product lines.

JOB SUMMARY

Company:

AYRTON Drug

Industry:

Pharmaceutical

Category:

Quality Assurance

Location:

Accra

Job Status:

Full-time

Salary:

GH¢ 

Education:

Undergraduate

Experience:

2 years

Job Expires:

10 Jun, 2013

Job Description

Reports to Managing Director

Scope: 
The role of Regulatory Affairs Executive is to ensure that the drug regulatory aspect of the business is well developed and maintained.

Responsibilities:

  • Develop registration strategies, prioritize assignments, co-ordinate regulatory projects and activities in accordance with the strategic objectives of the company
  • Review, analyze and co-ordinate data for new product submissions, line extensions and  variations to marketed products
  • Preparing regulatory documentation and dossiers
  • Keep accurate records on the usage of narcotic and psychotropic substances by the company, applying for narcotic licence and submission to appropriate bodies.
  • Ensure full regulatory compliance to all local and international regulations, codes and standards.
  • Liaising and building relationships with regulatory authorities
  • Writing clear, accessible product labels and patient information leaflets
  • Project managing teams of colleagues involved with the development of new products, variation of products, artwork designing and approvals.
  • Analyzing and communicating trends in regulatory legislation, guidelines and customer practices in all the countries that the company exports to and their implications to the company

Required Skills or Experience

  • University qualifications in Pharmacy or related Science discipline are essential.
  • At least 2 years experience with Drug Regulatory Affairs is preferred
  • Experience working on both local and foreign drug dossiers is preferred.
  • Competencies
  • Excellent communication skills
  • Ability to work and deliver results with very little supervision
  • Attention to detail
  • Excellent presentation and negotiation skills
  • Good organization and analytical skills
  • Equity statement
  • Ability to develop productive working relationships


NB: SALARY & BENEFITS :  VERY ATTRACTIVE

How To Apply

Interested applicants should send applications to include CV to:
 

adml2@hotmail.com  

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